PEONOVA is an AI clinical decision engine that reads guidelines, verifies eligibility, and structures treatment plans.
Request a DemoEvery treatment decision involves a chain of work that should never require a specialist. Reading through 300-page guidelines. Cross-checking SmPC criteria drug by drug. Manually piecing together fragmented patient records. Verifying eligibility step by step. It's not clinical work. But it's consuming clinical time.
80% of the work surrounding a treatment decision is administrative, repetitive, and guideline-driven. That's not a workflow problem. That's a structural one.
Clinical guidelines change constantly. Tracking them manually across NCCN, ESMO, EAU, and national frameworks is unsustainable at scale.
Every drug has its own eligibility criteria, contraindications, and reimbursement rules. Verifying them takes time clinicians don't have.
Patient data lives across discharge summaries, lab results, and imaging reports that are unstructured, scattered, and time-consuming to synthesize.
Chronic disease care doesn't end at the treatment plan. Monitoring, dose adjustments, and follow-up scheduling add compounding administrative load over months and years.
In healthcare, trust is not optional. A clinician won't act on a recommendation they can't trace. An institution won't adopt a system they can't audit. A regulator won't approve a black box.
We built PEONOVA on one principle: every output must be explainable. Not just what the system recommends — but which guideline rule was applied, which SmPC criterion was evaluated, and which patient data point triggered the logic. That's not a feature. That's the foundation.
PEONOVA doesn't replace clinical judgment. It structures everything around it.
PEONOVA ingests published clinical guidelines (NCCN, ESMO, EAU, national protocols) and converts them into structured logic. For each patient case, it generates all eligible treatment options, ranks them by suitability, and explains why each applies or doesn't.
Combined with treatment options, PEONOVA walks through every SmPC criterion indication alignment, contraindications, drug interactions, reimbursement rules. What typically takes hours of cross-referencing takes minutes. Flags are instant. Documentation is automatic.
PEONOVA assembles the clinical decision into a structured, reviewable treatment plan with guideline citations, eligibility assessments, and documented reasoning. Built for the clinician to approve, not to second-guess.
For chronic conditions, PEONOVA generates a living task timeline from guidelines and SmPC rules monitoring schedules, lab requirements, dose adjustment triggers, and follow-up milestones. The complexity stays inside the system. The clinician sees clear next steps and recommendations.
Complex cases resolved into evidence-ranked options in minutes, not hours of manual work.
Every option, plan, and action links back to the guideline section or SmPC rule that justified it.
Clinicians see the reasoning behind every recommendation. Explainable AI they can verify and trust.
Reduces clinical variability in long-term treatment pathways across patients, practitioners, and institutions.
PEONOVA handles the guideline complexity. Clinicians focus on the patient.
We started where the complexity is hardest - cancer. If the engine can handle it there, it can handle it anywhere. Cancer is the starting point. All of medicine is the scale.
Prostate cancer first. Then lung, kidney, breast, colorectal. The hardest test we could find. The engine passed.
Same engine. New guidelines loaded. The conditions consuming 80% of global healthcare spend, all addressable.
Every condition with a guideline is within reach. The zeros on the right are not a gap. They're where we're headed.
The engine is live, the reasoning is visible, and the impact on clinical time is real. We'd love to show you.
Request a Demo